A thioredoxin inhibitor
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Ferroptocide

Item No. 39005

Technical Information
Formal Name
(2S,3aS,4S,5R,7R,8S,8aS,9R)-octahydro-2,8a-dihydroxy-4,8,9-trimethyl-1-oxo-5-(2,3,5,8-tetrahydro-1,3-dioxo-2-phenyl-1H-[1,2,4]triazolo[1,2-a]pyridazin-6-yl)-1H-3a,8-propanoazulen-7-yl ester, 2-chloro-acetic acid
CAS Number
2505218-38-0
Molecular Formula
C30H36ClN3O7
Formula Weight
Purity
≥90%
Formulation
A solid
DMSO: SolubleMethanol: Soluble
SMILES
O=C(N1CC([C@H](C[C@@H](OC(CCl)=O)[C@]23C)[C@@H]([C@@]([C@]3(C([C@H]4O)=O)O)(C4)CC[C@H]2C)C)=CCN15)N(C6=CC=CC=C6)C5=O
InChi Code
InChI=1S/C30H36ClN3O7/c1-17-9-11-29-14-22(35)25(37)30(29,40)28(17,3)23(41-24(36)15-31)13-21(18(29)2)19-10-12-32-26(38)34(27(39)33(32)16-19)20-7-5-4-6-8-20/h4-8,10,17-18,21-23,35,40H,9,11-16H2,1-3H3/t17-,18+,21-,22+,23-,28+,29+,30-/m1/s1
InChi Key
LLYJISDUHFXOHK-GOCONZMPSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Ferroptocide is an inhibitor of thioredoxin (Trx) and a derivative of pleuromutilin (Item No. 19452).1 It inhibits Trx activity in ES-2 ovarian cancer cells when used at a concentration of 20 µM and is cytotoxic to ES-2 cells (IC50 = 1.6 µM). Ferroptocide (5 µM) induces ferroptosis in ES-2 cells, an effect that can be blocked by the iron chelator deferoxamine (DFO; Item No. 14595), antioxidant Trolox (Item No. 10011659), or ferroptosis inhibitor ferrostatin-1 (Item No. 17729). It decreases tumor volume in a 4T1 murine mammary carcinoma model using immunocompetent but not immunodeficient mice when administered at 50 mg/kg twice per week.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Llabani, E., Hicklin, R.W., Lee, H.Y., et alDiverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis. Nat. Chem. 11(6), 521-532 (2019).